WithdrawnNot Applicable

French Cohort of Patients With Rotator Cuff Lesions

Stopped: The sponsor, in consultation with the coordinating investigator, decided to stop the study prematurely on 01/10/2025. No patients were enrolled in the study.

0Started 2025-04

Plain-language summary

The purpose of this study is to identify, at 5 years, the clinical and therapeutic factors associated with improvement in shoulder functionality and quality of life in patients with transfixing (total) rotator cuff injuries undergoing treatment.

Who can participate

Age range18 Years – 75 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patient, male or female, over 18 years of age. * Patient with a transfixing (total) rotator cuff lesion confirmed by imaging. * A patient who has been informed and has expressed no oral objection to taking part in the research. * Patient affiliated to or benefiting from a social security scheme. Exclusion Criteria: * Patients over 75 years of age. * Patients with a history of shoulder surgery. * Patients unable to receive emails and/or answer online questionnaires. * Protected patient: adult under guardianship, curatorship or other legal protection, deprived of liberty by judicial or administrative decision.

What they're measuring

Shoulder Pain and Disability Index

Timeframe: 5 years

European quality of life scale - EQ5D

Timeframe: 5 years

Trial details

NCT IDNCT06371872

SponsorGCS Ramsay Santé pour l'Enseignement et la Recherche

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2035-12

View on ClinicalTrials.gov More Rotator Cuff Injuries trials